vitalwiki

Синдром Коффіна-Лоурі

ORPHA:192· ICD-10 Q87.0· Coffin-Lowry syndrome

Визначення(English summary)

A rare X-linked syndromic intellectual disability characterized by global development delay, postnatal growth retardation leading to short stature, facial dysmorphism, short hands with tapering fingers and progressive skeletal abnormalities including kyphoscoliosis and pectus carinatum/excavatum. Intellectual disability ranges from mild to severe.

Поширеність
1-9 / 100 000
Успадкування
X-linked dominant
Вік початку
Childhood, Infancy, Neonatal